BEDOPS v2.4.41

  • ← 3. Revision history
  • 4.1. Visualizing the relationship of SNPs and generic genomic features →
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4. Usage examples¶

The following examples demonstrate the use of BEDOPS in analyzing genomic data. Here, we provide source code and snippets of data to demonstrate “real-world” examples based on daily usage of these tools in the Stamatoyannopoulos lab.

  • 4.1. Visualizing the relationship of SNPs and generic genomic features
    • 4.1.1. BEDOPS tools in use
    • 4.1.2. Script
    • 4.1.3. Discussion
    • 4.1.4. Downloads
  • 4.2. Collapsing multiple BED files into a master list by signal
    • 4.2.1. BEDOPS tools in use
    • 4.2.2. Script
    • 4.2.3. Discussion
  • 4.3. Measuring the frequency of signed distances between SNPs and nearest DHSes
    • 4.3.1. BEDOPS tools in use
    • 4.3.2. Script
    • 4.3.3. Discussion
    • 4.3.4. Downloads
  • 4.4. Finding the subset of SNPs within DHSes
    • 4.4.1. BEDOPS tools in use
    • 4.4.2. Script
    • 4.4.3. Discussion
    • 4.4.4. Downloads
  • 4.5. Smoothing raw tag count data across the genome
    • 4.5.1. BEDOPS tools in use
    • 4.5.2. Script
  • 4.6. Efficiently creating Starch-formatted archives with a cluster
    • 4.6.1. BEDOPS tools in use
    • 4.6.2. Script
    • 4.6.3. Discussion
      • 4.6.3.1. Splitting BED files
      • 4.6.3.2. Compressing BED subsets
      • 4.6.3.3. Stitching together compressed sets
  • 4.7. Working with many input files at once with bedops and bedmap
    • 4.7.1. Discussion

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  • ← 3. Revision history
  • 4.1. Visualizing the relationship of SNPs and generic genomic features →
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